EP0184863B1 - Catalyseur tris(dimethylamino)sulphonium bifluorure - Google Patents
Catalyseur tris(dimethylamino)sulphonium bifluorure Download PDFInfo
- Publication number
- EP0184863B1 EP0184863B1 EP85201447A EP85201447A EP0184863B1 EP 0184863 B1 EP0184863 B1 EP 0184863B1 EP 85201447 A EP85201447 A EP 85201447A EP 85201447 A EP85201447 A EP 85201447A EP 0184863 B1 EP0184863 B1 EP 0184863B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- tris
- dimethylamino
- mmol
- sulfonium
- polymerization
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- IARSSOVWSJAVSZ-UHFFFAOYSA-N tris(dimethylamino)sulfanium Chemical compound CN(C)[S+](N(C)C)N(C)C IARSSOVWSJAVSZ-UHFFFAOYSA-N 0.000 title claims description 15
- 239000003054 catalyst Substances 0.000 title claims 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 11
- 238000006116 polymerization reaction Methods 0.000 claims description 11
- 239000000178 monomer Substances 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- HIHYQHFFHYZPMR-UHFFFAOYSA-N tris(diethylamino)sulfanium Chemical compound CCN(CC)[S+](N(CC)CC)N(CC)CC HIHYQHFFHYZPMR-UHFFFAOYSA-N 0.000 claims 1
- 229920000642 polymer Polymers 0.000 description 21
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 15
- -1 azide ions Chemical class 0.000 description 12
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 11
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 10
- 238000005227 gel permeation chromatography Methods 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 7
- 239000004926 polymethyl methacrylate Substances 0.000 description 7
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 229910052786 argon Inorganic materials 0.000 description 5
- 230000003197 catalytic effect Effects 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
- 229910052794 bromium Inorganic materials 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- ZOCHPFUNABVYOQ-UHFFFAOYSA-N trimethyl-[2-methyl-1-(2-trimethylsilyloxyethoxy)prop-1-enoxy]silane Chemical compound C[Si](C)(C)OC(=C(C)C)OCCO[Si](C)(C)C ZOCHPFUNABVYOQ-UHFFFAOYSA-N 0.000 description 3
- JNOGVQJEBGEKMG-UHFFFAOYSA-N (1-methoxy-2-methylprop-1-enoxy)-trimethylsilane Chemical compound COC(=C(C)C)O[Si](C)(C)C JNOGVQJEBGEKMG-UHFFFAOYSA-N 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 2
- AGPAALRHMDYOAD-UHFFFAOYSA-N 5-bromo-2,5-dimethylcyclohexa-1,3-diene Chemical compound CC1=CCC(C)(Br)C=C1 AGPAALRHMDYOAD-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 2
- AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 2
- 239000003426 co-catalyst Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- OKTJSMMVPCPJKN-OUBTZVSYSA-N Carbon-13 Chemical compound [13C] OKTJSMMVPCPJKN-OUBTZVSYSA-N 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 0 ON1N*CC=*1c1ccccc1 Chemical compound ON1N*CC=*1c1ccccc1 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 229910010066 TiC14 Inorganic materials 0.000 description 1
- 229910003074 TiCl4 Inorganic materials 0.000 description 1
- NFAXUNMUHPEKPU-UHFFFAOYSA-N [O-][Si]([O-])([O-])OC(F)F.CN(C)[S+](N(C)C)N(C)C.CN(C)[S+](N(C)C)N(C)C.CN(C)[S+](N(C)C)N(C)C Chemical compound [O-][Si]([O-])([O-])OC(F)F.CN(C)[S+](N(C)C)N(C)C.CN(C)[S+](N(C)C)N(C)C.CN(C)[S+](N(C)C)N(C)C NFAXUNMUHPEKPU-UHFFFAOYSA-N 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000000082 organogermanium group Chemical group 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920000120 polyethyl acrylate Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/12—Esters of monohydric alcohols or phenols
- C08F20/14—Methyl esters, e.g. methyl (meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/72—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from metals not provided for in group C08F4/44
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
- C08F293/005—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/06—Metallic compounds other than hydrides and other than metallo-organic compounds; Boron halide or aluminium halide complexes with organic compounds containing oxygen
- C08F4/12—Metallic compounds other than hydrides and other than metallo-organic compounds; Boron halide or aluminium halide complexes with organic compounds containing oxygen of boron, aluminium, gallium, indium, thallium or rare earths
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
Definitions
- This invention relates to tris(dimethylamino)sulfonium bifluoride having utility as a polymerization catalyst, and to a process for preparing such compound.
- Co-pending European Patent Application No. 82303405.3 (Publication No. 0 068 887), of which this Application is a Divisional, describes and claims a process of preparing a "living" polymer, the process comprising contacting under polymerizing conditions at least one polar acrylic-type or maleimide, alphaolefinic, monomer with (i) a tetra-coordinate organosilicon, organo-tin, or organo-germanium polymerization initiator containing at least one initiating site and (ii) a co-catalyst which is a source of bifluoride, fluoride, cyanide, or azide ions or a suitable Lewis acid.
- Such compound may be used as the source of bifluoride ions in the polymerization process of copending Application No. 82303405.3.
- tris(dimethylamino)sulfonium bifluoride is prepared by reacting a silicate of the formula wherein Me is as defined above, with water or a lower alkanol, for example, methanol; water is preferred since higher yields are obtained.
- the tris(dimethylamino)sulfonium difluoromethylsilicate which is used as starting material in the process of the present invention, can be prepared according to the processes disclosed by Middleton, U.S. Patent 3,940,402.
- This example illustrates the preparation of a "living" polymer which can further polymerize after more than 20 h. Polymerization is initiated by MTS in the presence of bifluoride ions as co-catalyst.
- hydroxy-terminated methyl methacrylate (35%)/n-butyl methacrylate (BMA) (65%) copolymer was prepared using the following amounts of materials: [(2-methyl-1-[2-(trimethylsiloxy)ethoxy]-1-propenyl)oxy]trimethylsilane, 0.51 g (1.85 mmol); MMA, 11 ml (103.7 mmol); BMA, 30 ml (188.5 mmol); tris(dimethylamino)sulfonium bifluoride, 20 mg (0.1 mmol); THF, 100 ml. Upon addition of the monomers the temperature rose to 48.6° from 20.6°. Evaporation of solvents and drying of the resultant residue gave 38.6 g of copolymer.
- GPC Mn 22100, M w 24500, D 1.11 (theor. M w 20,215).
- This example demonstrates the preparation of "living" poly(methyl methacrylate) containing active terminal trimethylsiloxy groups, and subsequent reactions thereof.
- the invention provides a catalytic compound for use in preparing useful and well known polymers containing functional substituents, for example, homopolymers and copolymers of acrylate and/or methacrylate monomers, such polymers heretofore being made usually by anionic polymerization techniques.
- the invention also provides a catalytic compound for use in making certain commercially desirable, relatively monodisperse copolymers of methacrylate and acrylate comonomers, such copolymers being difficult or impossible to obtain by known processes such as anionic polymerization or free-radical polymerization.
- the invention also provides a catalytic compound for use in making "living" polymer which may be cast or spun, for example, into a film or fiber, from solution (in an aprotic solvent) or isolated, processed, and then further polymerized.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Polymerization Catalysts (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Graft Or Block Polymers (AREA)
- Polymerisation Methods In General (AREA)
Claims (5)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT85201447T ATE53593T1 (de) | 1981-06-30 | 1982-06-29 | Tris(dimethylamino)-sulfonium-bifluoridkatalysator. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US27902581A | 1981-06-30 | 1981-06-30 | |
US279025 | 1981-06-30 |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP82303405.3 Division | 1982-06-29 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0184863A2 EP0184863A2 (fr) | 1986-06-18 |
EP0184863A3 EP0184863A3 (en) | 1986-10-22 |
EP0184863B1 true EP0184863B1 (fr) | 1990-06-13 |
Family
ID=23067360
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP82303405A Expired EP0068887B1 (fr) | 1981-06-30 | 1982-06-29 | Polymères vivantes et procédé de leur préparation |
EP85201447A Expired - Lifetime EP0184863B1 (fr) | 1981-06-30 | 1982-06-29 | Catalyseur tris(dimethylamino)sulphonium bifluorure |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP82303405A Expired EP0068887B1 (fr) | 1981-06-30 | 1982-06-29 | Polymères vivantes et procédé de leur préparation |
Country Status (18)
Country | Link |
---|---|
US (1) | US4681918A (fr) |
EP (2) | EP0068887B1 (fr) |
JP (1) | JPS5813603A (fr) |
KR (1) | KR890004083B1 (fr) |
AR (1) | AR241118A1 (fr) |
AT (1) | ATE53593T1 (fr) |
AU (1) | AU565180B2 (fr) |
BR (1) | BR8203809A (fr) |
DE (2) | DE3280190D1 (fr) |
DK (1) | DK165456C (fr) |
ES (1) | ES513604A0 (fr) |
GB (1) | GB2102818A (fr) |
HK (2) | HK47987A (fr) |
MX (1) | MX174590B (fr) |
NO (1) | NO158627C (fr) |
SG (1) | SG22387G (fr) |
ZA (1) | ZA824678B (fr) |
ZW (1) | ZW13282A1 (fr) |
Families Citing this family (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0127388B1 (fr) * | 1983-05-20 | 1986-12-30 | Ciba Specialty Chemicals Water Treatments Limited | Polymères solubles dans l'eau |
ES8607367A1 (es) * | 1983-11-07 | 1986-06-16 | Du Pont | Un procedimiento para fabricar una composicion de recubrimiento a base de polimeros hechos de monomeros alfaolefinicos polares. |
US4544724A (en) * | 1984-06-19 | 1985-10-01 | E. I. Du Pont De Nemours And Company | Silylated vinyl alcohol polymers |
AU583045B2 (en) * | 1984-07-05 | 1989-04-20 | E.I. Du Pont De Nemours And Company | Acrylic star polymers |
GB8419805D0 (en) * | 1984-08-03 | 1984-09-05 | Allied Colloids Ltd | Aqueous drilling and packer fluids |
JPH0618808B2 (ja) * | 1984-10-08 | 1994-03-16 | 日本合成ゴム株式会社 | ビニル系重合体の製法 |
GB8428985D0 (en) * | 1984-11-16 | 1984-12-27 | Allied Colloids Ltd | Water soluble polymers |
US4780554A (en) * | 1984-11-20 | 1988-10-25 | Union Carbide Corporation | O-silylated ketene acetals and enol ethers and method of preparation |
US4656233A (en) * | 1984-11-29 | 1987-04-07 | E. I. Du Pont De Nemours And Company | "Living" polymers and chain transfer-regulated polymerization process |
US4605716A (en) * | 1985-02-14 | 1986-08-12 | E. I. Du Pont De Nemours And Company | Lewis base-catalyzed polymerization |
CA1250997A (fr) * | 1985-03-01 | 1989-03-07 | Ira B. Dicker | Stimulation de la vie active d'un polymere dans la polymerisation avec un oxyanion comme catalyseur |
US4588795A (en) * | 1985-03-01 | 1986-05-13 | E. I. Du Pont De Nemours And Company | Oxyanion-catalyzed polymerization |
US4983679A (en) * | 1986-05-29 | 1991-01-08 | E. I. Dupont De Nemours And Company | β-(keto or sulfonyl)esters from reaction of silylketene acetal and acyl or sulfonyl compound |
US5260424A (en) * | 1986-05-29 | 1993-11-09 | E. I. Du Pont De Nemours And Company | B-(keto or sulfonyl) esters from reaction of silylketene acetal and acyl or sulfonyl compound |
US5110869A (en) * | 1986-05-29 | 1992-05-05 | E. I. Du Pont De Nemours And Company | β-(keto or sulfonyl)esters from reaction of silyketene acetal and acyl or sulfonyl compound |
US4822859A (en) * | 1986-06-10 | 1989-04-18 | E. I. Du Pont De Nemours And Company | Group transfer polymerization and initiators therefor |
US4957973A (en) * | 1986-07-08 | 1990-09-18 | E. I. Du Pont De Nemours And Company | Uncatalyzed process for preparing "living" polymers |
US4728706A (en) * | 1986-08-29 | 1988-03-01 | E. I. Du Pont De Nemours And Company | Titanium, zirconium- and hafnium containing initiators in the polymerization of acrylic monomers to "living" polymers |
AU7895387A (en) * | 1986-09-29 | 1988-03-31 | E.I. Du Pont De Nemours And Company | Living polymers from unsaturated si, sn or ge initiators |
US4732955A (en) * | 1986-09-29 | 1988-03-22 | E. I. Du Pont De Nemours And Company | Group transfer polymerization catalyzed by mercury compounds |
US4806605A (en) * | 1987-01-27 | 1989-02-21 | E. I. Du Pont De Nemours And Company | Monomers and initiators for group transfer polymerization |
GB8705277D0 (en) * | 1987-03-06 | 1987-04-08 | Jenkins A D | Preparing graft copolymers |
US4771116A (en) * | 1987-04-30 | 1988-09-13 | E. I. Du Pont De Nemours And Company | Silylamines as additives in group transfer polymerization |
EP0295401A3 (fr) * | 1987-04-30 | 1990-03-21 | Wacker-Chemie Gmbh | Procédé de polymérisation de composés polaires |
US4845156A (en) * | 1987-12-21 | 1989-07-04 | E. I. Du Pont De Nemours And Company | Preparation of macromonomers |
GB8730131D0 (en) * | 1987-12-24 | 1988-02-03 | Ici Plc | Catalysts |
US5019634A (en) * | 1988-02-16 | 1991-05-28 | E. I. Du Pont De Nemours And Company | Group transfer living polymer grafted to an initiator support |
GB8803765D0 (en) * | 1988-02-18 | 1988-03-16 | Ici Plc | Polymerisation process |
GB8803764D0 (en) * | 1988-02-18 | 1988-03-16 | Ici Plc | Polymerisation process |
US4866145A (en) * | 1988-04-01 | 1989-09-12 | E. I. Du Pont De Nemours And Company | Catalyst for group transfer polymerization |
US4943648A (en) * | 1988-04-01 | 1990-07-24 | E. I. Du Pont De Nemours And Company | Initiators for group transfer polymerization |
US5021524A (en) * | 1988-04-14 | 1991-06-04 | E. I. Du Pont De Nemours And Company | Initiator for group transfer polymerization |
US5187244A (en) * | 1988-07-22 | 1993-02-16 | Mitsubishi Rayon Co., Ltd. | Preparation process of block copolymers and resulting block copolymers |
JPH02140211A (ja) * | 1988-11-22 | 1990-05-29 | Nippon Oil & Fats Co Ltd | 分子内にペルオキシ給合を有するマレイミド系共重合体 |
US4906713A (en) * | 1989-01-31 | 1990-03-06 | E. I. Du Pont De Nemours And Company | "Acrylic" ladder polymers |
US4978723A (en) * | 1989-03-01 | 1990-12-18 | E. I. Du Pont De Nemours And Company | Phosphonate-capped polymers |
US4939211A (en) * | 1989-03-01 | 1990-07-03 | E. I. Du Pont De Nemours And Company | Phosphonate-capped polymers |
GB8914574D0 (en) * | 1989-06-24 | 1989-08-16 | Ici Plc | Catalysts |
GB8914575D0 (en) * | 1989-06-24 | 1989-08-16 | Ici Plc | Catalysts |
FR2649400B1 (fr) * | 1989-07-10 | 1993-01-08 | Norsolor Sa | Copolymeres en etoile et leur procede de fabrication |
US5244981A (en) * | 1990-04-10 | 1993-09-14 | Permeable Technologies, Inc. | Silicone-containing contact lens polymers, oxygen permeable contact lenses and methods for making these lenses and treating patients with visual impairment |
US5314960A (en) * | 1990-04-10 | 1994-05-24 | Permeable Technologies, Inc. | Silicone-containing polymers, oxygen permeable hydrophilic contact lenses and methods for making these lenses and treating patients with visual impairment |
US5371147A (en) * | 1990-10-11 | 1994-12-06 | Permeable Technologies, Inc. | Silicone-containing acrylic star polymers, block copolymers and macromonomers |
US5206295A (en) * | 1991-02-25 | 1993-04-27 | E. I. Du Pont De Nemours And Company | Coating composition comprising an anhydride-containing polymer and a structured epoxy-containing polymer |
EP0618956B1 (fr) * | 1991-12-23 | 2001-07-11 | Albemarle Corporation | Produits d'addition michael polyfonctionnels et compositions de refrigeration contenant lesdits produits |
DE4418647A1 (de) * | 1993-05-28 | 1994-12-01 | Kansai Paint Co Ltd | Wäßrige Harzdispersion |
US6943203B2 (en) * | 1998-03-02 | 2005-09-13 | Johnson & Johnson Vision Care, Inc. | Soft contact lenses |
US7619040B2 (en) * | 2002-02-15 | 2009-11-17 | Ppg Industries Ohio, Inc. | Compositions containing copolymers of olefinic monomers |
US20040143079A1 (en) * | 2003-01-21 | 2004-07-22 | Simion Coca | Compositions containing copolymers of isobutylene type monomers |
US6784248B2 (en) * | 2002-02-15 | 2004-08-31 | Ppg Industries Ohio, Inc. | Thermosetting compositions containing alternating copolymers of isobutylene type monomers |
WO2007008575A1 (fr) * | 2005-07-13 | 2007-01-18 | L'oreal | Compositions cosmetiques contenant des polymeres liposolubles et des agents donnant du collant |
US7884158B2 (en) * | 2005-09-06 | 2011-02-08 | L'Oré´al | Cosmetic compositions containing block copolymers, tackifiers and phenylated silicones |
EP3433288A1 (fr) * | 2016-03-22 | 2019-01-30 | Technische Universität München | Polymérisation de monomères de type michael |
EP3502094A1 (fr) | 2017-12-21 | 2019-06-26 | Covestro Deutschland AG | Procédé de fabrication de polyols téléchéliques à partir de trithiocarbonates |
TWI684607B (zh) * | 2018-09-20 | 2020-02-11 | 國立清華大學 | 嵌段共聚物及其製備方法 |
WO2020100591A1 (fr) * | 2018-11-15 | 2020-05-22 | 住友化学株式会社 | Article moulé et son procédé de production |
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GB1057998A (en) * | 1964-11-09 | 1967-02-08 | Kurashiki Rayon Kk | Process for the production of poly (methyl methacrylate) |
NL7113482A (fr) * | 1971-10-01 | 1973-04-03 | ||
US3940402A (en) * | 1974-09-19 | 1976-02-24 | E. I. Dupont De Nemours And Company | Tris(substituted amino) sulfonium salts |
JPS5837321B2 (ja) * | 1978-04-19 | 1983-08-16 | 東ソー株式会社 | アニオン重合方法 |
US4413084A (en) * | 1980-10-23 | 1983-11-01 | Ford Motor Company | Paint composition comprising hydroxy functional film former and improved stabilized flow control additive |
US4396680A (en) * | 1981-03-04 | 1983-08-02 | E. I. Du Pont De Nemours And Co. | Substrate coated with crater resistant acrylic enamel |
US4351924A (en) * | 1981-03-16 | 1982-09-28 | E. I. Du Pont De Nemours And Company | ω-, and α,ω-Hydroxyhydrocarbyl-(alkyl methacrylate) polymers and process |
US4417034A (en) * | 1981-06-30 | 1983-11-22 | E. I. Du Pont De Nemours & Co. | Living polymers and process for their preparation |
US4598161A (en) * | 1983-04-04 | 1986-07-01 | E. I. Du Pont De Nemours And Company | Tris(dialkylamino)sulfonium bifluoride catalysts |
-
1981
- 1981-11-21 US US06/673,926 patent/US4681918A/en not_active Expired - Lifetime
-
1982
- 1982-06-29 AT AT85201447T patent/ATE53593T1/de active
- 1982-06-29 EP EP82303405A patent/EP0068887B1/fr not_active Expired
- 1982-06-29 EP EP85201447A patent/EP0184863B1/fr not_active Expired - Lifetime
- 1982-06-29 DK DK292682A patent/DK165456C/da not_active IP Right Cessation
- 1982-06-29 DE DE8585201447T patent/DE3280190D1/de not_active Expired - Lifetime
- 1982-06-29 AU AU85442/82A patent/AU565180B2/en not_active Expired
- 1982-06-29 DE DE8282303405T patent/DE3273440D1/de not_active Expired
- 1982-06-29 GB GB08218808A patent/GB2102818A/en not_active Withdrawn
- 1982-06-29 KR KR8202894A patent/KR890004083B1/ko active
- 1982-06-29 JP JP57110922A patent/JPS5813603A/ja active Granted
- 1982-06-29 MX MX193368A patent/MX174590B/es unknown
- 1982-06-29 NO NO822230A patent/NO158627C/no unknown
- 1982-06-30 ES ES513604A patent/ES513604A0/es active Granted
- 1982-06-30 AR AR289857A patent/AR241118A1/es active
- 1982-06-30 ZW ZW132/82A patent/ZW13282A1/xx unknown
- 1982-06-30 ZA ZA824678A patent/ZA824678B/xx unknown
- 1982-06-30 BR BR8203809A patent/BR8203809A/pt not_active IP Right Cessation
-
1987
- 1987-03-04 SG SG223/87A patent/SG22387G/en unknown
- 1987-06-18 HK HK479/87A patent/HK47987A/xx not_active IP Right Cessation
-
1990
- 1990-10-03 HK HK804/90A patent/HK80490A/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
NO158627B (no) | 1988-07-04 |
KR890004083B1 (ko) | 1989-10-20 |
HK47987A (en) | 1987-06-26 |
AU565180B2 (en) | 1987-09-10 |
SG22387G (en) | 1987-07-10 |
NO158627C (no) | 1988-10-12 |
ES8307843A1 (es) | 1983-08-01 |
HK80490A (en) | 1990-10-12 |
ZA824678B (en) | 1984-03-28 |
ES513604A0 (es) | 1983-08-01 |
EP0184863A3 (en) | 1986-10-22 |
ATE53593T1 (de) | 1990-06-15 |
EP0068887B1 (fr) | 1986-09-24 |
JPS5813603A (ja) | 1983-01-26 |
BR8203809A (pt) | 1983-07-05 |
AR241118A1 (es) | 1991-11-15 |
NO822230L (no) | 1983-01-03 |
DK165456C (da) | 1993-04-19 |
DE3273440D1 (en) | 1986-10-30 |
DK165456B (da) | 1992-11-30 |
DK292682A (da) | 1982-12-31 |
DE3280190D1 (de) | 1990-07-19 |
GB2102818A (en) | 1983-02-09 |
AR241118A2 (es) | 1991-11-15 |
KR840000588A (ko) | 1984-02-25 |
AU8544282A (en) | 1983-01-06 |
EP0184863A2 (fr) | 1986-06-18 |
ZW13282A1 (en) | 1982-09-29 |
MX174590B (es) | 1994-05-27 |
EP0068887A1 (fr) | 1983-01-05 |
JPH0579685B2 (fr) | 1993-11-04 |
US4681918A (en) | 1987-07-21 |
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